FDA.reportPublic FDA data

REXALL

Manufacturer
DOLGENCORP INC | APOLLO HEALTH AND BEAUTY CARE
Effective date
2015-03-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:41:54

Label at a glance#

ProductREXALL PETROLEUM WITH VITAMIN E AND ALOE
Active ingredientPETROLATUM
Label structure6 sections

Dosage and administration

APPLY AS NEEDED

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

PETROLATUM 99.8%

PURPOSE

OTC - PURPOSE SECTION

SKIN PROTECTANT

USE

INDICATIONS & USAGE SECTION

  • TEMPORARILY PROTECTS MINOR:
  • CUTS
  • SCRAPES
  • BURNS
  • TEMPORARILY PROTECTS AND HELPS RELIEVE CHAPPED OR CRACKED SKIN AND LIPS
  • HELPS PROTECT FROM THE DRYING EFFECTS OF WIND AND COLD WEATHER

WARNINGS

WARNINGS SECTION

FOR EXTERNAL USE ONLY

WHEN USING THIS PRODUCT

OTC - WHEN USING SECTION

DO NOT GET INTO EYES

STOP USE AND ASK A DOCTOR IF

OTC - STOP USE SECTION

CONDITIONS LASTS MORE THAN 7 DAYS

DO NOT USE ON

OTC - DO NOT USE SECTION

  • DEEP PUNCTURE WOUNDS
  • ANIMAL BITES
  • SERIOUS BURNS
KEEP OUT OF REACH OF CHIDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

APPLY AS NEEDED

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

ALOE BARBADENSIS LEAF JUICE, FRAGRANCE (PARFUM), TOCOPHERYL ACETATE

LABEL COPY

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

IMAGE OF THE LABELIMAGE OF THE LABEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1100455petrolatum 99.8 % Topical GelPSN1
1100455petrolatum 0.998 MG/MG Topical GelSCD1
1100455petrolatum 99.8 % Topical GelSY1
1100455petrolatum 99.8 % Topical JellySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55910-316-132020-01-31C16284748780-19d75b9cf-d748-f424-e053-dadaa90a57ceDRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55910-316-13REXALLPETROLEUM WITH VITAMIN E AND ALOE368 g in 1 JARJELLY3681

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55910-316REXALL PETROLEUM WITH VITAMIN E AND ALOE (PETROLATUM) JELLY [DOLGENCORP INC]1Legacy NDC, 1 package rows20150305_b1c5a1aa-3c7b-4efb-a86a-85dc5ff95bad.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
PETROLATUMACTIVE INGREDIENT4T6H12BN9U1
PETROLATUMACTIVE MOIETY4T6H12BN9U1
.ALPHA.-TOCOPHEROL ACETATEINACTIVE INGREDIENT9E8X80D2L01
ALOE VERA LEAFINACTIVE INGREDIENTZY81Z83H0X1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55910-31655910-316-13

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
PETROLATUM4T6H12BN9UACTIB
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 3 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
.ALPHA.-TOCOPHEROL ACETATE.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0FILM / BUCCAL0.09 mgExact identifier — unii candidate
3 equally ranked IID candidates
.ALPHA.-TOCOPHEROL ACETATE.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0CAPSULE / ORAL2 mgExact identifier — unii candidate
3 equally ranked IID candidates
.ALPHA.-TOCOPHEROL ACETATE.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0TABLET / ORAL0.5 mgExact identifier — unii candidate
3 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
6f40df2a-edd8-4fd9-ba17-d568daf32d45b1c5a1aa-3c7b-4efb-a86a-85dc5ff95bad2015-03-04WarningsExact identifier
spl id: 6f40df2a-edd8-4fd9-ba17-d568daf32d45
spl set id: b1c5a1aa-3c7b-4efb-a86a-85dc5ff95bad

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.